US6323219B1
Expired / Lapsed
US
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Methods for treating immunomediated inflammatory disorders
Assignee: Janssen Pharmaceuticals Inc
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Filing: 1999-01-27
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Granted: 2001-11-27
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Expires: 2019-01-27
Abstract
Abstract This invention relates to methods ands compositions for bringing about changes in skin pigmentation and for treating inflammatory disorders. More particularly, this invention relates to compounds which affect melanogenesis and can be used as depigmenting agents or as agents for darkening skin utilizing the PAR-2 pathway and compounds for the, prevention and treatment of immunomediated inflammatory diseases, particularly those associated with the respiratory tract, such as asthma and allergic rhinitis.
Inventors
- 👤 Michael J. Costanzo
Bibliographic Details
Application Number
—
Jurisdiction
US
Data Source
google_patents
Last Synchronized
2026-11-09 14:19
CPC Classifications
A; A61; A61Q; A61Q19/00; A61Q19/04; A61K; A61K8/00; A61K8/02; A61K8/14; A61K8/18; A61K8/30; A61K8/40; A61K8/41; A61K8/42; A61K8/44; A61K8/46; A61K8/49; A61K8/4906; A61K8/4926; A61K8/64; A61K8/67; A61K8/676; A61K8/678; A61K8/96; A61K8/97; A61K8/9783; A61K8/9789; A61Q19/02
Claims Analysis
Total Claims: 22
Claim 1
Independent Claim
1715 words
A method of treating an inflammatory disorder in a subject in need thereof comprising administering to the patient a therapeutically effective amount of a compound of formula (I) wherein: A is selected from the group consisting of C 1-8 alkyl, carboxyC 1-4 alkyl, C 1-4 alkoxycarbonyC 1-4 alkyl, phenylC 1-4 alkyl, substituted phenylC 1-4 alkyl (where the phenyl substituents are independently selected from one or more of, C 1-4 alkyl, perfluoroC 1-4 alkyl, C 1-4 alkoxy, hydroxy, halo, amido, nitro, amino, C 1-4 alkylamino, C 1-4 dialkylamino, carboxy or C 1-4 alkoxycarbonyl), formyl, C 1-4 alkoxycarbonyl, C 1-2 alkylcarbonyl, phenylC 1-4 alkoxycarbonyl, C 3-7 cycloalkylcarbonyl, phenylcarbonyl, substituted phenylcarbonyl (where the phenyl substituents are independently selected from one or more of, C 1-4 alkyl, perfluoroC 1-4 alkyl, C 1-4 alkoxy, hydroxy, halo, amido, nitro, amino, C 1-4 alkylamino, C 1-4 dialkylamino, carboxy or C 1-4 alkoxycarbonyl), C 1-4 alkylsulfonyl, C 1-4 alkoxysulfonyl, perfluoroC 1-4 alkylsulfonyl, phenylsulfonyl, substituted phenylsulfonyl (where the phenyl substituents are independently selected from one or more of, C 1-4 alkyl, perfluoroC 1-4 alkyl, C 1-4 alkoxy, hydroxy, halo, amido, nitro, amino, C 1-4 alkylamino, C 1-4 dialkylamino, carboxy or C 1-4 alkoxycarbonyl), 10-camphorsulfonyl, phenylC 1-4 alkylsulfonyl, substituted phenylC 1-4 alkylsulfonyl, C 1-4 alkylsulfinyl, perfluoroC 1-4 alkylsulfinyl, phenylsulfinyl, substituted phenylsulfinyl (where the phenyl substituents are independently selected from one or more of, C 1-4 alkyl, perfluoroC 1-4 alkyl, C 1-4 alkoxy, hydroxy, halo, amido, nitro, amino, C 1-4 alkylamino, C 1-4 dialkylamino, carboxy or C 1-4 alkoxycarbonyl), phenylC 1-4 alkylsulfinyl, substituted phenylC 1-4 alkylsulfinyl, 1-naphthylsulfonyl, 2-naphthylsulfonyl or substituted naphthylsulfonyl (where the naphthyl substituents are independently selected from one or more of, C 1-4 alkyl, perfluoroC 1-4 alkyl, C 1-4 alkoxy, hydroxy, halo, amido, nitro, amino, carboxy or C 1-4 alkoxycarbonyl ), 1-naphthylsulfinyl, 2-naphthylsulfinyl or substituted naphthylsulfinyl (where the naphthyl substituents are independently selected from one or more of, C 1-4 alkyl, perfluoroC 1-4 alkyl, C 1-4 alkoxy, hydroxy, halo, amido, nitro, amino, C 1-4 alkylamino, C 1-4 dialkylamino, carboxy or C 1-4 alkoxycarbonyl); a D or L amino acid which is coupled at its carboxy terminus to the nitrogen depicted in formula I and is selected from the group consisting of alanine, asparagine, 2-azetidinecarboxylic acid, glycine, N-C 1-8 alkylglycine, proline, 1-amino-1 -cycloC 3-8 alkylcarboxylic acid, thiazolidine-4-carboxylic acid, 5,5-dimethylthiazolidine-4-carboxylic acid, oxazolidine-4-carboxylic acid, pipecolinic acid, valine, methionine, cysteine, serine, threonine, norleucine, leucine, tert-leucine, isoleucine, phenylalanine, 1 -naphthalanine, 2-naphthalanine, 2-thienylalanine, 3-thienylalanine, [1,2,3,4]-tetrahydroisoquinoline-1-carboxylic acid and [1,2,3,4]-tetrahydroisoquinoline-2-carboxylic acid where the amino terminus of said amino acid is connected to a member selected from the group consisting of C 1-4 alkyl, tetrazol-5-yl-C 1-2 alkyl, carboxyC 1-4 alkyl, C 1-4 alkoxycarbonylC 1-4 alkyl, phenylC 1-4 alkyl, substituted phenyl C 1-4 alkyl (where the phenyl substituents are independently selected from one or more of, C 1-4 alkyl, perfluoroC 1-4 alkyl, C 1-4 alkoxy, hydroxy, halo, amido, nitro, amino, C 1-4 alkylamino, C 1-4 dialkylamino, carboxy or C 1-4 alkoxycarbonyl), 1,1-diphenylC 1-4 alkyl, 3-phenyl-2-hydroxypropionyl, 2,2-diphenyl-1-hydroxyethylcarbonyl, [1,2,3,4]-tetrahydroisoquinoline-1-carbonyl, [1,2,3,4]-tetrahydroisoquinoline-3-carbonyl, 1 -methylamino-1-cyclohexanecarbonyl, 1-hydroxy-1-cyclohexanecarbonyl, 1-hydroxy-1-phenylacetyl, 1-cyclohexyl-1-hydroxyacetyl, 3-phenyl-2-hydroxypropionyl, 3,3-diphenyl-2-hydroxypropionyl, 3-cyclohexyl-2-hydroxypropionyl, formyl, C 1-4 alkoxycarbonyl, C 1-2 alkylcarbonyl, perfluoroC 1-4 alkylC 0-4 alkylcarbonyl, phenylC 1-4 alkylcarbonyl, substituted phenylC 1-4 alkylcarbonyl (where the phenyl substituents are independently selected from one or more of, C 1-4 alkyl, perfluoroC 1-4 alkyl, C 1-4 alkoxy, hydroxy, halo, amido, nitro, amino, C 1-4 alkylamino, C 1-4 dialkylamino, carboxy or C 1-4 alkoxycarbonyl) 1,1-diphenylC 1-4 alkylcarbonyl, substituted 1,1-diphenylC 1-4 alkylcarbonyl (where the phenyl substituents are independently selected from one or more of, C 1-4 alkyl, perfluoro C 1-4 alkyl, C 1-4 alkoxy, hydroxy, halo, amido, nitro, amino, C 1-4 alkylamino, C 1-4 alkylamino, carboxy or C 1-4 alkoxycarbonyl), perfluoroC 1-4 alkylsulfonyl, C 1-4 alkylsulfonyl, C 1-4 alkoxysulfonyl, phenylsulfonyl, substituted phenylsulfonyl (where the phenyl substituents are independently selected from one or more of, C 1-4 alkyl, perfluoro C 1-4 alkyl, C 1-4 alkoxy, hydroxy, halo, amido, nitro, amino, C 1-4 alkylamino, C 1-4 dialkylamino, carboxy or C 1-4 alkoxycarbonyl), 10-camphorsulfonyl, phenylC 1-4 alkylsulfonyl, substituted phenylC 1-4 alkylsulfonyl, perfluoroC 1-4 alkylsulfinyl, C 1-4 alkylsulfinyl, phenylsulfinyl, substituted phenylsulfinyl (where the phenyl substituents are independently selected from one or more of, C 1-4 alkyl, perfluoro C 1-4 alkyl, C 1-4 alkoxy, hydroxy, halo, amido, nitro, amino, C 1-4 alkylamino, C 1-4 dialkylamino, carboxy or C 1-4 alkoxycarbonyl), phenylC 1-4 alkylsulfinyl, substituted phenylC 1-4 alkylsulfinyl (where the phenyl substituents are independently selected from one or more of, C 1-4 alkyl, perfluoro C 1-4 alkyl, C 1-4 alkoxy, hydroxy, halo, amido, nitro, amino, C 1-4 alkylamino, C 1-4 dialkylamino, carboxy or C 1-4 -alkoxycarbonyl), 1-naphthylsulfonyl 2-naphthylsulfonyl, substituted naphthylsulfonyl (where the naphthyl substituents are independently selected from one or more of, C 1-4 alkyl, perfluoroC 1-4 alkyl, C 1-4 alkoxy, hydroxy, halo, amido, nitro, amino, C 1-4 alkylamino, C 3-4 dialkylamino, carboxy or C 1-4 -alkoxycarbonyl), 1-naphthylsulfinyl, 2-naphthylsulfinyl, and substituted naphthylsulfinyl (where the naphthyl substituents are independently selected from one or more of, C 1-4 alkyl, perfluoroC 1-4 alkyl, C 1-4 alkoxy, hydroxy, halo, amido, nitro, amino, C 1-4 alkylamino, C 1-2 -dialkylamino, carboxy or C 1-4 alkoxycarbonyl); or a poly peptide comprised of two amino acids, where the first amino acid is a D or L amino acid, bound via its carboxy terminus to the nitrogen depicted in formula I and is selected from the group consisting of glycine, N-C 1-8 alkylglycine, alanine, 2-azetidinecarboxylic acid, proline, thiazolidine-carboxylic acid, 5,5-dimethylthiazolidine-4-carboxylic acid, oxazolidine-4-carboxylic acid, 1-amino-1-cycloC 3-8 alkylcarboxylic acid, 3-hydroxyproline, 4-hydroxyproline, 3-(C 1-4 alkoxy)proline, 4-(C 1-4 -alkoxy)proline, 3,4-dehydroproline, 2,2-dimethyl-4-thiazolidine carboxylic acid, 2,2-dimethyl-4-oxazolidine carboxylic acid, pipecolinic acid, valine, methionine, cysteine, asparagine, serine, threonine, leucine, tert-leucine, isoleucine, phenylalanine, 1-naphthalanine, 2-naphthalanine, 2-thienylalanine, 3-thienylalanine, [1,2,3,4]-tetrahydroisoquinoline-1-carboxylic acid, [1,2,3,4]-tetrahydroisoquinoline-2-carboxylic acid, aspartic acid-4-C 1-4 alkyl ester and glutamic acid-5-C 1-4 alkyl ester and the second D or L amino acid, is bound to the amino terminus of said first amino acid, and is selected from the group consisting of phenylalanine, 4-benzoylphenylalanine, 4-carboxyphenylalanine, 4-(carboxy C 0-2 alkyl)phenylalanine, substituted phenylalanine (where the phenyl substituents are independently selected from one or more of, C 1-4 alkyl, perfluoroC 1-4 alkyl, C 1-4 alkoxy, hydroxy, halo, amido, nitro, amino, C 1-4 alkylamino, C 1-4 dialkylamino, carboxy or C 1-4 alkoxycarbonyl), 3-benzothienylalanine, 4-biphenylalanine, homophenylalanine, octahydroindole-2-carboxylic acid, 2-pyridylalanine, 3-pyridylalanine, 4-thiazolyalanine, 2-thienylalanine, 3-(3-benzothienyl)alanine, 3-thienylalanine, tryptophan, tyrosine, asparagine, 3-tri-C 1-4 alkylsilylalanine, cyclohexylglycine, diphenyiglycine, phenylglycine, methionine sulfoxide, methionine sulfone, 2,2-dicyclohexylalanine, 2-(1-naphthylalanine), 2-(2-naphthylalanine), phenyl substituted phenylalanine (where the substituents are selected from C 1-4 alkyl, perfluoroC 1-4 alkyl, C 1-4 alkoxy, hydroxy, halo, amido, nitro, amino, C 1-4 alkylamino, C 1-4 dialkylamino, carboxy or C 1-4 alkoxycarbonyl), aspartic acid, aspartic acid-4-C 1-4 alkyl ester, glutamic acid, glutamic acid-5-C 1-4 alkyl ester, cycloC 3-8 alkylalanine, substituted cycloC 3-8 alkylalanine (where the ring substituents are carboxy, C 1-4 alkylcarboxy, C 1-4 alkoxycarbonyl or aminocarbonyl), 2,2-diphenylalanine and all alpha-C 1-5 alkyl of all amino acid derivatives thereof, where the amino terminus of said second amino acid is unsubstituted or monosubstituted with a member of the group consisting of formyl, C 1-12 alkyl, tetrazol-5-ylC 1-2 alkyl, carboxyC 1-8 alkyl, carboalkoxyC 1-4 alkyl, phenyl C 1-4 alkyl, substituted phenylC 1-4 alkyl (where the phenyl substituents are independently selected from one or more of, C 1-4 alkyl, perfluoroC 1-4 alkyl, C 1-4 alkoxy, hydroxy, halo, amido, nitro, amino, C 1-4 alkylamino, C 1-4 dialkylamino, carboxy or C 1-4 alkoxycarbonyl), 1,1-diphenylC 1-4 alkyl, C 1-6 alkoxycarbonyl, phenylC 1-6 alkoxycarbonyl, C 1-12 alkylcarbonyl, perfluoroC 1-4 alkylC 0-4 alkylcarbonyl, phenylC 1-4 alkylcarbonyl, substituted phenylC 1-4 alkylcarbonyl (where the phenyl substituents are independently selected from one or more of, C 1-4 alkyl, perfluoro C 1-4 alkyl, C 1-4 alkoxy, hydroxy, halo, amido, nitro, amino, C 1-4 alkylamino, C 1-4 dialkylamino, carboxy or C 1-4 alkoxycarbonyl), 1,1-diphenylC 1-4 alkylcarbonyl, C 1-4 alkylsulfonyl, C 1-4 alkoxysulfonyl, perfluoroC 1-4 alkylsulfonyl, phenylsulfonyl, substituted phenylsufonyl (where the phenyl substituents are independently selected from one or more of, C 1-4 alkyl, perfluoroC 1-4 alkyl, C 1-4 alkoxy, hydroxy, halo, amido, nitro, amino, C 1-4 alkylamino, C 1-4 dialkylamino, carboxy or C 1-4 alkoxycarbonyl), 10-camphorsulfonyl, phenylC 1-4 alkylsulfonyl, substituted phenylC 1-4 alkylsulfonyl, C 1-4 alkylsulfinyl, perfluoro C 1-4 alkylsulfinyl, phenylsulfinyl, substituted phenylsufinyl (where the phenyl substituents are independently selected from one or more of, C 1-4 alkyl, perfluoroC 1-4 alkyl, C 1-4 alkoxy, hydroxy, halo, amido, nitro, amino, C 1-4 alkylamino, C 1-4 dialkylamino, carboxy or C 1-4 alkoxycarbonyl), phenylC 1-4 alkylsulfinyl, substituted phenylC 1-4 alkylsulfinyl 1-naphthylsulfonyl, 2-naphthylsulfonyl, substituted naphthylsulfonyl (where the naphthyl substituent is selected from C 1-4 alkyl, perfluoroC 1-4 alkyl, C 1-4 alkoxy, hydroxy, halo, amido, nitro, amino, C 1-4 alkylamino, C 1-4 dialkylamino, carboxy or C 1-4 alkoxycarbonyl), 1-naphthylsulfinyl, 2-naphthylsulfinyl and substituted naphthylsulfinyl (where the naphthyl substituent is selected from C 1-4 alkyl, perfluoroC 1-4 alkyl, C 1-4 alkoxy, hydroxy, halo, amido, nitro, amino, C 1-4 alkylamino, C 1-4 dialkylamino, carboxy or C 1-4 alkoxycarbonyl); R 1 is selected from the group consisting of hydrogen and C 1-5 alkyl. R 2 is selected from the group consisting of aminoC 2-5 alkyl, guanidinoC 2-5 alkyl, C 1-4 alkylguanidinoC 2-5 alkyl, diC 1-4 alkylguanidinoC 2-5 alkyl, amidinoC 2-5 alkyl, C 1-4 alkylamidinoC 2-5 alkyl, diC 1-4 alkylamidinoC 2-5 alkyl, C 1-3 alkoxy C 2-5 alkyl, phenyl, substituted phenyl (where the substituents are independently selected from one or more of, amino, amidino, guanidino, C 1-4 alkylamino, C 1-4 dialkylamino, halogen, perfluoro C 1-4 alkyl, C 1-4 alkyl, C 1-3 alkoxy or nitro), benzyl, phenyl substituted benzyl (where the substituents are independently selected from one or more of, amino, amidino, guanidino, C 1-4 alkylamino, C 1-4 dialkylamino, halogen, perfluoro C 1-4 alkyl, C 1-4 alkyl, C 1-3 alkoxy or nitro), hydroxyC 2-5 alkyl, C 1-5 alkylaminoC 2-5 alkyl, C 2-5 dialkylaminoC 2-5 alkyl, 4-aminocyclohexylC 0-2 alkyl and C 1-5 alkyl; p is 0 or 1 B is where n is 0-3, R3 is H or C 1-5 alkyl and the carbonyl moiety of B is bound to E; E is a heterocycle selected from the group consisting of oxazolin-2-yl, oxazol-2-yl, thiazol-2-yl, thiazol-5-yl, thiazol-4-yl, thiazolin-2-yl, imidazol-2-yl, 4-oxo-2-quinoxalin-2-yl, 2-pyridyl, 3-pyridyl, benzo[b]thiophen-2-yl, benzoxazol-2-yl, benzimidazol-2-yl, benzothiazol-2-yl, triazol-4-yl, triazol-6-yl, tetrazol-2-yl pyrimidin-2-yl, quinolin-2-yl, indol-2-yl, pyrazol-2-yl, 4,5,6,7-tetrahydrobenzothiazol-2-yl, naphtho[2,1-d]thiazol-2-yl, naphtho[1,2d]thiazol-2-yl quinoxalin-2-yl, isoquinolin-1-yl, isoquinolin-3-yl, benzo[b]furan-2-yl, pyrazin-2-yl, quinazolin-2-yl, isothiazol-5-yl, isothiazol-3-yl, purin-8-yl and a substituted heterocycle where the substituents are independently selected from C 1-4 alkyl, perfluoro C 1-4 alkyl, C 1-4 alkoxy, hydroxy, halo, amido, nitro, amino, C 1-4 alkylamino, C 1-4 dialkylamino, carboxy, C 1-4 alkoxycarbonyl, hydroxy or phenylC 1-4 alkylaminocarbonyl; and pharmaceutically acceptable salts and prodrugs thereof.
Claim 2
Independent Claim
1715 words
A method of treating an inflammatory disorder in a subject in need thereof comprising administering to the patient a therapeutically effective amount of a compound of formula (I) wherein: A is selected from the group consisting of C 1-8 alkyl, carboxyC 1-4 alkyl, C 1-4 alkoxycarbonyC 1-4 alkyl, phenylC 1-4 alkyl, substituted phenylC 1-4 alkyl (where the phenyl substituents are independently selected from one or more of, C 1-4 alkyl, perfluoroC 1-4 alkyl, C 1-4 alkoxy, hydroxy, halo, amido, nitro, amino, C 1-4 alkylamino, C 1-4 dialkylamino, carboxy or C 1-4 alkoxycarbonyl), formyl, C 1-4 alkoxycarbonyl, C 1-2 alkylcarbonyl, phenylC 1-4 alkoxycarbonyl, C 3-7 cycloalkylcarbonyl, phenylcarbonyl, substituted phenylcarbonyl (where the phenyl substituents are independently selected from one or more of, C 1-4 alkyl, perfluoroC 1-4 alkyl, C 1-4 alkoxy, hydroxy, halo, amido, nitro, amino, C 1-4 alkylamino, C 1-4 dialkylamino, carboxy or C 1-4 alkoxycarbonyl), C 1-4 alkylsulfonyl, C 1-4 alkoxysulfonyl, perfluoroC 1-4 alkylsulfonyl, phenylsulfonyl, substituted phenylsulfonyl (where the phenyl substituents are independently selected from one or more of, C 1-4 alkyl, perfluoroC 1-4 alkyl, C 1-4 alkoxy, hydroxy, halo, amido, nitro, amino, C 1-4 alkylamino, C 1-4 dialkylamino, carboxy or C 1-4 alkoxycarbonyl), 10-camphorsulfonyl, phenylC 1-4 alkylsulfonyl, substituted phenylC 1-4 alkylsulfonyl, C 1-4 alkylsulfinyl, perfluoroC 1-4 alkylsulfinyl, phenylsulfinyl, substituted phenylsulfinyl (where the phenyl substituents are independently selected from one or more of, C 1-4 alkyl, perfluoroC 1-4 alkyl, C 1-4 alkoxy, hydroxy, halo, amido, nitro, amino, C 1-4 alkylamino, C 1-4 dialkylamino, carboxy or C 1-4 alkoxycarbonyl), phenylC 1-4 alkylsulfinyl, substituted phenylC 1-4 alkylsulfinyl, 1-naphthylsulfonyl, 2-naphthylsulfonyl or substituted naphthylsulfonyl (where the naphthyl substituents are independently selected from one or more of, C 1-4 alkyl, perfluoroC 1-4 alkyl, C 1-4 alkoxy, hydroxy, halo, amido, nitro, amino, carboxy or C 1-4 alkoxycarbonyl ), 1-naphthylsulfinyl, 2-naphthylsulfinyl or substituted naphthylsulfinyl (where the naphthyl substituents are independently selected from one or more of, C 1-4 alkyl, perfluoroC 1-4 alkyl, C 1-4 alkoxy, hydroxy, halo, amido, nitro, amino, C 1-4 alkylamino, C 1-4 dialkylamino, carboxy or C 1-4 alkoxycarbonyl); a D or L amino acid which is coupled at its carboxy terminus to the nitrogen depicted in formula I and is selected from the group consisting of alanine, asparagine, 2-azetidinecarboxylic acid, glycine, N-C 1-8 alkylglycine, proline, 1-amino-1 -cycloC 3-8 alkylcarboxylic acid, thiazolidine-4-carboxylic acid, 5,5-dimethylthiazolidine-4-carboxylic acid, oxazolidine-4-carboxylic acid, pipecolinic acid, valine, methionine, cysteine, serine, threonine, norleucine, leucine, tert-leucine, isoleucine, phenylalanine, 1 -naphthalanine, 2-naphthalanine, 2-thienylalanine, 3-thienylalanine, [1,2,3,4]-tetrahydroisoquinoline-1-carboxylic acid and [1,2,3,4]-tetrahydroisoquinoline-2-carboxylic acid where the amino terminus of said amino acid is connected to a member selected from the group consisting of C 1-4 alkyl, tetrazol-5-yl-C 1-2 alkyl, carboxyC 1-4 alkyl, C 1-4 alkoxycarbonylC 1-4 alkyl, phenylC 1-4 alkyl, substituted phenyl C 1-4 alkyl (where the phenyl substituents are independently selected from one or more of, C 1-4 alkyl, perfluoroC 1-4 alkyl, C 1-4 alkoxy, hydroxy, halo, amido, nitro, amino, C 1-4 alkylamino, C 1-4 dialkylamino, carboxy or C 1-4 alkoxycarbonyl), 1,1-diphenylC 1-4 alkyl, 3-phenyl-2-hydroxypropionyl, 2,2-diphenyl-1-hydroxyethylcarbonyl, [1,2,3,4]-tetrahydroisoquinoline-1-carbonyl, [1,2,3,4]-tetrahydroisoquinoline-3-carbonyl, 1 -methylamino-1-cyclohexanecarbonyl, 1-hydroxy-1-cyclohexanecarbonyl, 1-hydroxy-1-phenylacetyl, 1-cyclohexyl-1-hydroxyacetyl, 3-phenyl-2-hydroxypropionyl, 3,3-diphenyl-2-hydroxypropionyl, 3-cyclohexyl-2-hydroxypropionyl, formyl, C 1-4 alkoxycarbonyl, C 1-2 alkylcarbonyl, perfluoroC 1-4 alkylC 0-4 alkylcarbonyl, phenylC 1-4 alkylcarbonyl, substituted phenylC 1-4 alkylcarbonyl (where the phenyl substituents are independently selected from one or more of, C 1-4 alkyl, perfluoroC 1-4 alkyl, C 1-4 alkoxy, hydroxy, halo, amido, nitro, amino, C 1-4 alkylamino, C 1-4 dialkylamino, carboxy or C 1-4 alkoxycarbonyl) 1,1-diphenylC 1-4 alkylcarbonyl, substituted 1,1-diphenylC 1-4 alkylcarbonyl (where the phenyl substituents are independently selected from one or more of, C 1-4 alkyl, perfluoro C 1-4 alkyl, C 1-4 alkoxy, hydroxy, halo, amido, nitro, amino, C 1-4 alkylamino, C 1-4 alkylamino, carboxy or C 1-4 alkoxycarbonyl), perfluoroC 1-4 alkylsulfonyl, C 1-4 alkylsulfonyl, C 1-4 alkoxysulfonyl, phenylsulfonyl, substituted phenylsulfonyl (where the phenyl substituents are independently selected from one or more of, C 1-4 alkyl, perfluoro C 1-4 alkyl, C 1-4 alkoxy, hydroxy, halo, amido, nitro, amino, C 1-4 alkylamino, C 1-4 dialkylamino, carboxy or C 1-4 alkoxycarbonyl), 10-camphorsulfonyl, phenylC 1-4 alkylsulfonyl, substituted phenylC 1-4 alkylsulfonyl, perfluoroC 1-4 alkylsulfinyl, C 1-4 alkylsulfinyl, phenylsulfinyl, substituted phenylsulfinyl (where the phenyl substituents are independently selected from one or more of, C 1-4 alkyl, perfluoro C 1-4 alkyl, C 1-4 alkoxy, hydroxy, halo, amido, nitro, amino, C 1-4 alkylamino, C 1-4 dialkylamino, carboxy or C 1-4 alkoxycarbonyl), phenylC 1-4 alkylsulfinyl, substituted phenylC 1-4 alkylsulfinyl (where the phenyl substituents are independently selected from one or more of, C 1-4 alkyl, perfluoro C 1-4 alkyl, C 1-4 alkoxy, hydroxy, halo, amido, nitro, amino, C 1-4 alkylamino, C 1-4 dialkylamino, carboxy or C 1-4 -alkoxycarbonyl), 1-naphthylsulfonyl 2-naphthylsulfonyl, substituted naphthylsulfonyl (where the naphthyl substituents are independently selected from one or more of, C 1-4 alkyl, perfluoroC 1-4 alkyl, C 1-4 alkoxy, hydroxy, halo, amido, nitro, amino, C 1-4 alkylamino, C 3-4 dialkylamino, carboxy or C 1-4 -alkoxycarbonyl), 1-naphthylsulfinyl, 2-naphthylsulfinyl, and substituted naphthylsulfinyl (where the naphthyl substituents are independently selected from one or more of, C 1-4 alkyl, perfluoroC 1-4 alkyl, C 1-4 alkoxy, hydroxy, halo, amido, nitro, amino, C 1-4 alkylamino, C 1-2 -dialkylamino, carboxy or C 1-4 alkoxycarbonyl); or a poly peptide comprised of two amino acids, where the first amino acid is a D or L amino acid, bound via its carboxy terminus to the nitrogen depicted in formula I and is selected from the group consisting of glycine, N-C 1-8 alkylglycine, alanine, 2-azetidinecarboxylic acid, proline, thiazolidine-carboxylic acid, 5,5-dimethylthiazolidine-4-carboxylic acid, oxazolidine-4-carboxylic acid, 1-amino-1-cycloC 3-8 alkylcarboxylic acid, 3-hydroxyproline, 4-hydroxyproline, 3-(C 1-4 alkoxy)proline, 4-(C 1-4 -alkoxy)proline, 3,4-dehydroproline, 2,2-dimethyl-4-thiazolidine carboxylic acid, 2,2-dimethyl-4-oxazolidine carboxylic acid, pipecolinic acid, valine, methionine, cysteine, asparagine, serine, threonine, leucine, tert-leucine, isoleucine, phenylalanine, 1-naphthalanine, 2-naphthalanine, 2-thienylalanine, 3-thienylalanine, [1,2,3,4]-tetrahydroisoquinoline-1-carboxylic acid, [1,2,3,4]-tetrahydroisoquinoline-2-carboxylic acid, aspartic acid-4-C 1-4 alkyl ester and glutamic acid-5-C 1-4 alkyl ester and the second D or L amino acid, is bound to the amino terminus of said first amino acid, and is selected from the group consisting of phenylalanine, 4-benzoylphenylalanine, 4-carboxyphenylalanine, 4-(carboxy C 0-2 alkyl)phenylalanine, substituted phenylalanine (where the phenyl substituents are independently selected from one or more of, C 1-4 alkyl, perfluoroC 1-4 alkyl, C 1-4 alkoxy, hydroxy, halo, amido, nitro, amino, C 1-4 alkylamino, C 1-4 dialkylamino, carboxy or C 1-4 alkoxycarbonyl), 3-benzothienylalanine, 4-biphenylalanine, homophenylalanine, octahydroindole-2-carboxylic acid, 2-pyridylalanine, 3-pyridylalanine, 4-thiazolyalanine, 2-thienylalanine, 3-(3-benzothienyl)alanine, 3-thienylalanine, tryptophan, tyrosine, asparagine, 3-tri-C 1-4 alkylsilylalanine, cyclohexylglycine, diphenyiglycine, phenylglycine, methionine sulfoxide, methionine sulfone, 2,2-dicyclohexylalanine, 2-(1-naphthylalanine), 2-(2-naphthylalanine), phenyl substituted phenylalanine (where the substituents are selected from C 1-4 alkyl, perfluoroC 1-4 alkyl, C 1-4 alkoxy, hydroxy, halo, amido, nitro, amino, C 1-4 alkylamino, C 1-4 dialkylamino, carboxy or C 1-4 alkoxycarbonyl), aspartic acid, aspartic acid-4-C 1-4 alkyl ester, glutamic acid, glutamic acid-5-C 1-4 alkyl ester, cycloC 3-8 alkylalanine, substituted cycloC 3-8 alkylalanine (where the ring substituents are carboxy, C 1-4 alkylcarboxy, C 1-4 alkoxycarbonyl or aminocarbonyl), 2,2-diphenylalanine and all alpha-C 1-5 alkyl of all amino acid derivatives thereof, where the amino terminus of said second amino acid is unsubstituted or monosubstituted with a member of the group consisting of formyl, C 1-12 alkyl, tetrazol-5-ylC 1-2 alkyl, carboxyC 1-8 alkyl, carboalkoxyC 1-4 alkyl, phenyl C 1-4 alkyl, substituted phenylC 1-4 alkyl (where the phenyl substituents are independently selected from one or more of, C 1-4 alkyl, perfluoroC 1-4 alkyl, C 1-4 alkoxy, hydroxy, halo, amido, nitro, amino, C 1-4 alkylamino, C 1-4 dialkylamino, carboxy or C 1-4 alkoxycarbonyl), 1,1-diphenylC 1-4 alkyl, C 1-6 alkoxycarbonyl, phenylC 1-6 alkoxycarbonyl, C 1-12 alkylcarbonyl, perfluoroC 1-4 alkylC 0-4 alkylcarbonyl, phenylC 1-4 alkylcarbonyl, substituted phenylC 1-4 alkylcarbonyl (where the phenyl substituents are independently selected from one or more of, C 1-4 alkyl, perfluoro C 1-4 alkyl, C 1-4 alkoxy, hydroxy, halo, amido, nitro, amino, C 1-4 alkylamino, C 1-4 dialkylamino, carboxy or C 1-4 alkoxycarbonyl), 1,1-diphenylC 1-4 alkylcarbonyl, C 1-4 alkylsulfonyl, C 1-4 alkoxysulfonyl, perfluoroC 1-4 alkylsulfonyl, phenylsulfonyl, substituted phenylsufonyl (where the phenyl substituents are independently selected from one or more of, C 1-4 alkyl, perfluoroC 1-4 alkyl, C 1-4 alkoxy, hydroxy, halo, amido, nitro, amino, C 1-4 alkylamino, C 1-4 dialkylamino, carboxy or C 1-4 alkoxycarbonyl), 10-camphorsulfonyl, phenylC 1-4 alkylsulfonyl, substituted phenylC 1-4 alkylsulfonyl, C 1-4 alkylsulfinyl, perfluoro C 1-4 alkylsulfinyl, phenylsulfinyl, substituted phenylsufinyl (where the phenyl substituents are independently selected from one or more of, C 1-4 alkyl, perfluoroC 1-4 alkyl, C 1-4 alkoxy, hydroxy, halo, amido, nitro, amino, C 1-4 alkylamino, C 1-4 dialkylamino, carboxy or C 1-4 alkoxycarbonyl), phenylC 1-4 alkylsulfinyl, substituted phenylC 1-4 alkylsulfinyl 1-naphthylsulfonyl, 2-naphthylsulfonyl, substituted naphthylsulfonyl (where the naphthyl substituent is selected from C 1-4 alkyl, perfluoroC 1-4 alkyl, C 1-4 alkoxy, hydroxy, halo, amido, nitro, amino, C 1-4 alkylamino, C 1-4 dialkylamino, carboxy or C 1-4 alkoxycarbonyl), 1-naphthylsulfinyl, 2-naphthylsulfinyl and substituted naphthylsulfinyl (where the naphthyl substituent is selected from C 1-4 alkyl, perfluoroC 1-4 alkyl, C 1-4 alkoxy, hydroxy, halo, amido, nitro, amino, C 1-4 alkylamino, C 1-4 dialkylamino, carboxy or C 1-4 alkoxycarbonyl); R 1 is selected from the group consisting of hydrogen and C 1-5 alkyl. R 2 is selected from the group consisting of aminoC 2-5 alkyl, guanidinoC 2-5 alkyl, C 1-4 alkylguanidinoC 2-5 alkyl, diC 1-4 alkylguanidinoC 2-5 alkyl, amidinoC 2-5 alkyl, C 1-4 alkylamidinoC 2-5 alkyl, diC 1-4 alkylamidinoC 2-5 alkyl, C 1-3 alkoxy C 2-5 alkyl, phenyl, substituted phenyl (where the substituents are independently selected from one or more of, amino, amidino, guanidino, C 1-4 alkylamino, C 1-4 dialkylamino, halogen, perfluoro C 1-4 alkyl, C 1-4 alkyl, C 1-3 alkoxy or nitro), benzyl, phenyl substituted benzyl (where the substituents are independently selected from one or more of, amino, amidino, guanidino, C 1-4 alkylamino, C 1-4 dialkylamino, halogen, perfluoro C 1-4 alkyl, C 1-4 alkyl, C 1-3 alkoxy or nitro), hydroxyC 2-5 alkyl, C 1-5 alkylaminoC 2-5 alkyl, C 2-5 dialkylaminoC 2-5 alkyl, 4-aminocyclohexylC 0-2 alkyl and C 1-5 alkyl; p is 0 or 1 B is where n is 0-3, R3 is H or C 1-5 alkyl and the carbonyl moiety of B is bound to E; E is a heterocycle selected from the group consisting of oxazolin-2-yl, oxazol-2-yl, thiazol-2-yl, thiazol-5-yl, thiazol-4-yl, thiazolin-2-yl, imidazol-2-yl, 4-oxo-2-quinoxalin-2-yl, 2-pyridyl, 3-pyridyl, benzo[b]thiophen-2-yl, benzoxazol-2-yl, benzimidazol-2-yl, benzothiazol-2-yl, triazol-4-yl, triazol-6-yl, tetrazol-2-yl pyrimidin-2-yl, quinolin-2-yl, indol-2-yl, pyrazol-2-yl, 4,5,6,7-tetrahydrobenzothiazol-2-yl, naphtho[2,1-d]thiazol-2-yl, naphtho[1,2d]thiazol-2-yl quinoxalin-2-yl, isoquinolin-1-yl, isoquinolin-3-yl, benzo[b]furan-2-yl, pyrazin-2-yl, quinazolin-2-yl, isothiazol-5-yl, isothiazol-3-yl, purin-8-yl and a substituted heterocycle where the substituents are independently selected from C 1-4 alkyl, perfluoro C 1-4 alkyl, C 1-4 alkoxy, hydroxy, halo, amido, nitro, amino, C 1-4 alkylamino, C 1-4 dialkylamino, carboxy, C 1-4 alkoxycarbonyl, hydroxy or phenylC 1-4 alkylaminocarbonyl; and pharmaceutically acceptable salts and prodrugs thereof.
Claim 3
Dependent Claim
302 words
The method of claim 1 , wherein the compound has the formula wherein A is selected from C 4-8 cycloalkylcarbonyl, 1-naphthylsulfonyl, 2-naphthylsulfonyl, and substituted naphthylsulfonyls (where the substituents are selected from C 1-4 alkyl, perfluoroC 1-4 alkyl, C 1-4 alkoxy, hydroxy, halo, amido, nitro, amino, C 1-4 alkylamino, C 1-4 dialkylamino, carboxy and C 1-4 alkoxycarbonyl); an L amino acid such as glycine or proline, where the amino terminus is unsubstituted or monosubstituted with a member of the group consisting of 1-naphthylsulfonyl, 2-naphthylsulfonyl and substituted naphthylsulfonyls (where the substituents are selected from C 1-4 alkyl, perfluoroC 1-4 alkyl, C 1-4 alkoxy, hydroxy, halo, amido, nitro, amino, C 1-4 alkylamino, C 1-4 dialkylamino, carboxy and C 1-4 alkoxycarbonyl), formyl, and phenylcarbonyl; or a poly peptide comprised of two amino acids, where the first acid is L-proline or L-pipecolinic acid and the second acid is D-phenylalanine, D-cyclohexylalanine, D-diphenylalanine, methionine sulfone or (2,3,4,5,6-pentafluorophenyl)alanine where the amino terminus of said second amino acid is unsubstituted or monosubstituted with a member of the group consisting of C 1-5 alkyl, perfluoroC 1-4 -alkyl, phenylC 1-4 alkylsulfonyl or formyl; R 1 is selected from hydrogen or methyl; R 2 is selected from aminoC 2-5 alkyl, guanidinoC 2-5 alkyl, amidinoC 2-5 alkyl, benzyl, C 1-5 alkylaminoC 2-5 alkyl, C 1-5 dialkylaminoC 2-5 alkyl, 4-aminocyclohexylC 0-2 alkyl, 3-aminocyclohexylC 0-2 alkyl, C 1-5 alkoxyC 2-5 alkyl or C 1-5 alkyl; E is a heterocycle selected from thiazol-2-yl, thiazol-5-yl, thiazol-4-yl, thiazolin-2-yl, benzoxazol-2-yl, benzimidazol-2-yl, imidazol-2-yl, 4-oxo-2-quinoxalin-2-yl, benzothiazol-2-yl, triazol-4-yl, triazol-6-yl, tetrazol-2-yl, pyrimidin-2-yl, quinolin-2-yl, pyrazol-2-yl, [4,5,6,7]-tetrahydrobenzothiazol-2-yl, naphtho[2,1-d]thiazol-2-yl, naphtho[1,2-d]thiazol-2-yl, quinazolin-2-yl, isothiazol-5-yl, isothiazol-3-yl, purin-8-yl or a substituted heterocycle where the substituents are selected from C 1-4 alkyl, perfluoro C 1-4 alkyl, C 1-4 alkoxy, hydroxy, halo, amido, nitro, amino, C 1-4 alkylamino, C 1-4 dialkylamino, carboxy, C 1-4 alkoxycarbonyl or hydroxy; and pharmaceutically acceptable salts and prodrugs thereof.
Claim 4
Dependent Claim
193 words
The method of claim 2 wherein the compound has the formula wherein A is selected from C 4-8 cycloalkylcarbonyl; an L amino acid such as glycine or proline, where the amino terminus is unsubstituted or monosubstituted with a member of the group consisting of 1-naphthylsulfonyl, 2-naphthylsulfonyl and substituted naphthylsulfonyls (where the substituents are selected from C 1-4 alkyl, perfluoroC 1-4 alkyl, C 1-4 alkoxy, hydroxy, halo, amido, nitro, amino, C 1-4 alkylamino, C 1-4 dialkylamino, carboxy and C 1-4 alkoxycarbonyl), formyl, and phenylcarbonyl; or a poly peptide comprised of two amino acids, where the first acid is L-proline or L-pipecolinic acid and the second acid is D-phenylalanine, D-cyclohexylalanine, D-diphenylalanine, methionine sulfone or (2,3,4,5,6-pentafluorophenyl)alanine where the amino terminus of said second amino acid is unsubstituted or monosubstituted with a member of the group consisting of C 1-5 alkyl, perfluoroC 1-4 alkyl, phenylC 1-4 alkylsulfonyl or formyl; E is selected from benzothiazol-2-yl or substituted benzothiazol-2-yl where the substituents are selected from C 1-4 alkyl, perfluoro C 1-4 alkyl, C 1-4 alkoxy, hydroxy, halo, amido, nitro, amino, C 1-4 alkylamino, C 1-4 dialkylamino, carboxy, C 1-4 alkoxycarbonyl or hydroxy; and pharmaceutically acceptable salts and prodrugs thereof.
Claim 5
Dependent Claim
49 words
The method of claim 3 , wherein the compound has the formula wherein R 2 is selected from guanidinoC 2-5 alkyl, benzyl, C 1-5 alkoxyC 2-5 alkyl or C 1-5 alkyl; R 4 is selected from hydrogen, halo or C 1-4 alkoxycarbonyl; and pharmaceutically acceptable salts and prodrugs thereof.
Claim 6
Dependent Claim
19 words
The method of claim 4 , wherein the compound is selected from and pharmaceutically acceptable salts and prodrugs thereof.
Claim 7
Dependent Claim
15 words
The method of claim 1 , wherein the inflammatory disorder is an immunomediated inflammatory disorder.
Claim 8
Dependent Claim
66 words
The method of claim 6 , wherein the immunomediated inflammatory disorder is selected from asthma, allergic rhinitis, rheumatoid arthritis, rheumatoid spondylitis, osteoarthritis, gouty arthritis, arthritic conditions in general, peptic ulcers, ocular and vernal conjunctivitis, inflammatory bowel disease, Crohn's disease, urticaria, bullous pemphigoid, schleroderma, fibrosis, dermatitis, psoriasis, angioedema, eczematous dermatitis, analphylaxis, hyper proliferative skin disease, inflammatory skin conditions, hepatic cirrhosis, glomerulonephritis, nephritis, vascular inflammation, atherosclerosis, or restenosis.
Claim 9
Dependent Claim
17 words
The method of claim 6 , wherein the immunomediated inflammatory disorder is a mast-cell mediated inflammatory disorder.
Claim 10
Dependent Claim
19 words
The method of claim 8 , wherein the mast-cell mediated inflammatory disorder is selected from asthma or allergic rhinitis.
Claim 11
Dependent Claim
14 words
The method of claim 9 , wherein the mast-cell mediated inflammatory disorder is asthma.
Claim 12
Dependent Claim
21 words
The method of claim 7 , wherein the therapeutically effective amount of the compound is about 0.001 to about 2000 mg/kg/day.
Claim 13
Dependent Claim
21 words
The method of claim 11 , wherein the therapeutically effective amount of the compound is about 0.001 to about 200 mg/kg/day.
Claim 14
Dependent Claim
15 words
The method of claim 5 , wherein the inflammatory disorder is an immunomediated inflammatory disorder.
Claim 15
Dependent Claim
17 words
The method of claim 13 , wherein the immunomediated inflammatory disorder is a mast-cell mediated inflammatory disorder.
Claim 16
Dependent Claim
19 words
The method of claim 14 , wherein the mast-cell mediated inflammatory disorder is selected from asthma or allergic rhinitis.
Claim 17
Dependent Claim
14 words
The method of claim 15 , wherein the mast-cell mediated inflammatory disorder is asthma.
Claim 18
Dependent Claim
13 words
The method of claim 16 wherein the compound is administered as an aerosol.
Claim 19
Dependent Claim
23 words
The method of claim 16 wherein the compound is administered in combination with a β-adrenergic agonist, a methylxanthine, a cromoglycate or a corticosteroid.
Claim 20
Dependent Claim
49 words
The method of claim 18 wherein the β-adrenergic agonist is selected from albuterol, terbutaline, formoterol, fenoterol or prenaline; the methylxanthine is selected from caffeine, theophylline, aminophylline or theobromine; the cromoglycate is selected from cromolyn or nedocromil; and the corticosteroid is selected from beclomethasome, triamcinolone, flurisolide, dexamethasone, hydrocortisone or prednisone.
Claim 21
Dependent Claim
15 words
The method of claim 1 , wherein the compound is administered as a pharmaceutical composition.
Claim 22
Dependent Claim
36 words
The method of claim 20 wherein the pharmaceutical composition comprises a therapeutically effective amount of the compound of the formula I in a pharmaceutically acceptable carrier suitable for topical, oral, suppository, intranasal, inhalation or parenteral administration.
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